Function of CD14 as a peptidoglycan receptor: differences and similaritieswith LPS

Citation
R. Dziarski et D. Gupta, Function of CD14 as a peptidoglycan receptor: differences and similaritieswith LPS, J ENDOTOX R, 5(1-2), 1999, pp. 56-61
Citations number
44
Categorie Soggetti
Immunology
Journal title
JOURNAL OF ENDOTOXIN RESEARCH
ISSN journal
09680519 → ACNP
Volume
5
Issue
1-2
Year of publication
1999
Pages
56 - 61
Database
ISI
SICI code
0968-0519(1999)5:1-2<56:FOCAAP>2.0.ZU;2-Z
Abstract
Peptidoglycan (PGN) is a macrophage activator from Gram-positive bacteria. PGN activates cells of hemopoietic origin through CD14 since: (i) PGN-unres ponsive CD14-negative cells become PGN-responsive after transfection with C D14 and expression of membrane CD14; (ii) PGN binds to CD14 with high affin ity; and (iii) anti-CD14 mAbs inhibit both binding of PGN to CD14 and activ ation of CD14-positive cells by PCN. However, there are several differences in the function of CD14 as PGN and LPS receptor: (i) the kinetics of bindi ng are different; (ii) the affinity of binding in the absence of LPS-bindin g protein (LBP) is higher for PGN than LPS; (iii) LBP does not increase the affinity of binding of PGN to CD14 and does not enhance cell activation by PGN tin contrast to LPS); (iv) the regions of CD14 needed for binding and activation are partially similar and partially different for PGN and LPS; ( v) sCD14:PGN complexes, in contrast to sCD14:LPS complexes, do not activate CD14-negative cells; (vi) PGN, in contrast to LPS, does not activate CHO c ells expressing mCD14; and (vii) PGN and LPS induce differential activation of MAP kinases, but activate similar transcription factors (NF-kappa B, AT F1/CREB, and AP-1).